STAC3 related congenital myopathy: A case series of seven Comorian patients

Author:

Gromand Marie,Gueguen Paul,Pervillé Anne,Ferroul Fanny,Morel Godelieve,Harouna Anrifati,Doray Bérénice,Urtizberea J. Andoni,Alessandri Jean-Luc,Robin Stéphanie

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference25 articles.

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4. D'Arcy, C. E., Bjorksten, A., Yiu, E. M., Bankier, A., Gillies, R., McLean, C. A., Shield, L. K., Ryan, M. M. King-Denborough syndrome caused by a novel mutation in the ryanodine receptor gene. 2008. Neurology 71, 776-777.

5. Bringing together linguistic and genetic evidence to test the Bantu expansion;De Filippo;Proc. Biol. Sci.,2012

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